Ectd Jobs

Telix Pharmaceuticals is hiring a seasoned Medical Writer to lead and produce regulatory and clinical documentation for global submissions supporting its oncology and rare‑disease radiopharmaceutical portfolio.

SOKOL GxP Services seeks a hybrid Technical Writer to prepare and manage CMC regulatory submission content for a cell therapy clinical portfolio in New Brunswick, NJ.

Lead global regulatory strategy and submissions for device and combination products at AbbVie to enable timely approvals and ensure regulatory compliance.

Experienced Regulatory Affairs professional needed to lead preparation and coordination of regional regulatory submissions and labeling for investigational and commercial products at Gilead in Foster City.

Lead regulatory strategy and submissions for device and combination products at AbbVie to ensure timely global approvals and compliance.

Experienced CDISC/SDTM/ADaM programmer needed to lead FDA submission conformance reviews and provide regulatory guidance for submission-ready clinical data packages.

Lead device and combination product regulatory strategy and submissions at AbbVie to support timely approvals and market access.

Senior medical writer and team lead role responsible for authoring regulatory submissions and maturing medical writing processes at a growth-stage biotech focused on immunology.